Process for breaking petroleum emulsions



. Patented Sept. 7, 1943 PROCESS FOREBREAKIN G PETROLEUM MULSIONS Gwynne Allen, Long Beach, Calif., assignor to Petrolite Corporation, Ltd., St. Louis, Mo., a

corporation of Delaware No Drawing. Application May 2'7, 1942, Serial No. 444,766

13 Claims.

This invention relates primarily to the treatment of emulsions of mineral oil and water, such as petroleum emulsions, for the purpose of separating the oil from the water.

This invention is a continuation in part of my copending application, Serial No. 392,099, filed on May 6, 1941. Reference is also made to my copending applications Serial Numbers 444,761,

444,762, 444,763, 444,764, 444,765, and 444,767,.

filed May 27, 1942.

One object of my invention is to provide a novel process for resolving petroleum emulsions of the water-in-oil type that are commonly referred to as fcut oil, roily oil, emulsified oil, etc., and which comprise fine droplets of naturally-occurring waters or brines dispersed in a more or less permanent state throughout the oil which constitutes the continuous phase of the emulsion, my process being particularly adapted to the resolution of crude oil emulsions of the kind obtained in connection with the treatment or the flooding of subterranean oil-bearing strata by means of aqueous agents or the like.

Another object of my invention is to provide an economical and rapid process for separating emulsions which have been prepared under controlled conditions from mineral oil, such as crude petroleum and relatively soft waters or weak brines. Controlled emulsiflcation and subsequent demulsification under the conditions just mentioned are of significant value in removing i'mpurities, particularly inorganic salts, from pipeline oil.

The process which constitutes one feature of my present invention consists in subjecting a Detroleum emulsion of the water-in-oil type to the chain or radical. Where the oleic acid is employed in combination with a polyhydric alco-. hol, such as glycerol, as for example-in trlolein' which is the tri-glyceride of oleic acid, the reaction apparently does not stop with the formation of a simple addition product. Instead, as discussed in the literature, e. g., Knight and Stamberger, J. Chem. Soc. London, 1928, pp.

- 2791-8, triolein takes up additional sulfur atoms,

action of a demulsifying agent, thereby '.causing' radicals derived from unsaturated high molal mono-carboxylic detergent-forming acids having at least 8, and not more than 32, carbon atoms each.

It is known that when elemental sulfur is heated with a reactive detergent-forming carboxylic acid, for example with oleic acid, the sulfur adds at the double bond in the oleic acid possibly even tied in through the glyceryl radical. Also, it is probable that the several fatty acid radicals present are also linked through sulfur atoms. Compare comparable reactions involving more reactive sulfur di-chloride, and particularly the formation of cyclic bisulfides. Such reactions indicate the rationale for thioglycerol formation, or more exactly the formation of sulfurized esters of thioglycerol. See Chemistry of Synthetic Resins, Ellis, 1935, volume 2, 1176-77. At any rate, in the course of the reaction polymers begin to be formed and a certain degree of elasticity becomes apparent. Molecular weight determinations show the presence of polymers, including -diads and triads (dimers, trimers), etc. Destruction of the polymeric body, for example by saponification with'alkali, results in a reduction of the molecular weight, loss of the elastic properties, and apparently a return to a 'simpler addition product. In my process, I make no claim to the use of the simple unpolymerized addition product of sulfur and an unsaturated high molal monocarboxylic detergentforming acid having at least 8, and not more than 32, carbon atoms, typified 'by sulfurized oleic acid. I make no claim to the use of the free detergent-forming carboxylic acid'and sulfur alone in preparing my reagent; but I employ the acid only in combination with a polyhydric alcohol compound containing two or more alcoholiform hydroxyl groups, in the form of an ester of such acid and such polyhydric alcohol.

Thev compound containing the two or. more alcoholiform hydroxyl groups may be a simple polyhydric alcohol, such, for example, as glycerol or ethylene glycol, or it may be a condensed polyhydric alcohol like polyglycerol, di-ethylene glycol, di-glycerol, or tri-glycerol. In addition to the above polyhydric alcohols, I may also use mannitan, sorbitan, pentaerythritol, and dipentaerythritol. I may use ether alcohols so long as they have two or more hydroxyl groups in Y the molecule, i. e. (polyhydric alcohols in which a carbon atom chain is interrupted at least once by oxygen, as exemplified by di-ethylene glycol previously mentioned). They are all characterized by containing two or more alcoholiform hydroxyl groups and by having the power to form esters with an unsaturated high molal monocarboxylic detergent-forming acid having at least 8, and not more than 32, carbon atoms.

Resinous and similar materials are sometimes classified as thermoplastic, thermo-setting," and element convertible. The expression element-convertible refers particularly to plastic coatings or drying oils in which hardening apparently is due to conversion into a new compound or composition by action of an element used, often oxygen. Thus, drying oils are often referred to as being oxygen-convertible." For practical purposes, the only other element finding wide application for this purpose is sulfur. Hence, certain products, and particularly certain oils, are referred to as sulfur-convertible, meaning that they react with sulfur or sulfur dichloride to get polymeric materials, rubbery masses, factice, or the like.

The unsaturated high molal detergent-forming monocarboxylic acids employed by me in preparing my reagent are characterized by having a carbon atom chain, which I shall denote as R, containing at least 8 carbon atoms and not more than 32 carbon atoms, and which must contain at least one unsaturated bond, 1. e., at least one ethylene linkage. Such acids are sometimes referred to as ethylenic.

The acyl radical may, of course, have present other non-functional groups, such as hydroxyl groups, acyl-oxy groups, etc. It is only necessary that the presence of such groups does not detract from (a) the detergent-forming ability of the acids and (b) their susceptibility to sulfur conversion. Suitability of substituted acids is indicated by Very simple tests. For instance, saponification with caustic potash, caustic soda, or the like, must yield a soap or soap-like material. Secondly, if the detergent-forming properties have not been eliminated by the presence of this substituent atom or radical, then it is only necessary to determine that susceptibility to sulfur conversion is still present. Such test is obviously the same procedure as is herein described for preparing my reagent, except that it is conducted on a small scale'in the laboratory. If the substituted acid or ester which has been previously determined to have detergent-forming properties also shows sulfur conversion susceptility, it is, of course, the obvious functional equivalent of the unsubstituted or unmodified acids or esters herein described, and may be used with equal or even greater effectiveness.

Such high molal acids may be obtained from various sources, such as oils, fats, and waxes; or one may use petroleum acids, rosin acids, and the like. Petroleum acids include naturally-occurring naphthenic acids and also acids obtained by the oxidation of hydrocarbons and waxes. Rosin acids include abietic acid, p oabietic acids, and the like. Saturated acids, such as saturated fatty acids, saturated naphthenic acids, saturated oxidized petroleum acids, etc can frequently be converted into an unsaturated acid by halogenization, followed by a reaction of the kind exemplified by the internal Wurtz reaction.

My preference, of course, is to use unsaturated fatty acids, due to their low cost and ready availability. One need not use a single fatty acid, but may use the mixture employed by saponiflcation of a naturally-occurring oil or fat. For instance, special reference is made to the fatty acids which occur naturally in olive oil, castor oil, peanut oil, cottonseed oil, fish oils, corn oil, soybean oil, linseed oil, sesame oil, lard oil, oleo oil, Perilla oil, and many other naturally-occurring oils. Rapeseed oil, for example, contains appreciable proportions of tri-erucin, the tri-glyceride of erucic acid. I have found it useful to prepare my reagent.

As has been previously pointed out, the high molal acids are used in the form of the polyhydric alcohol ester having at least 2 such high molal acid radicals present. Since it is my preference to use the naturally-occurring fatty acids, it obviously follows that my preference is to use the naturally-occurring glycerides. However, if

desired, one can obtain the high molal acids from any source and esterify such acids with various polyhydric alcohols, such as the glycols, in the conventional manner to produce suitable esters which may or may not have a free or unreacted alcoholiform hydroxyl group present. The fatty acid di-glycerides typify these esters which contain a free or unreacted alcoholiform hydroxyl group (in the residue of the polyhydric alcohol, glycerol). The fatty acid tri-glycerides do not possess this free alcoholiform hydroxyl. Both types of glyceride, for example, are suitable for my purpose, provided the fatty acid present satisfies the above-expressed requirements. The manufacture of such esters is so well known that no description is required in the present instance.

One may select esters of the mixed type and such mixed esters may even contain acyl radicals which either are not high molal in character or are not unsaturated, i. e., ethylenic in nature. For instance, diolein may be reacted with one mol of acetic acid or one mol of ste'aric acid to give an ester which would be satisfactory for the present purpose. As an example of a modified ester which may serve, reference is made to triacetylated triricinolein.

In those instances where an ester of a high molal detergent-forming acid of the type previously described is first reacted with a polycarboxylic acid, before any other step in the preparation of my reagent, possession of one or more alcoholiform hydroxyl groups is required to confer reactivity. If the ester be a tri-glyceride, for example, the detergent-forming acid must contain an alcoholiform hydroxyl group. Ricinoleic acid would satisfy the requirement in this case. If the ester be a di-glyceride, the free alcoholiform hydroxyl group present in the glyceryl radical is sufficient to permit the di-glyceride to meet the above requirement.

I have found that, in addition to naturallyoccurring fatty acids, addition and substitution products of fatty acidswhich latter modified fatty acids bear a simple genetic relationship to the parent fatty acids from which they were derived-are also useful for making my reagent, so long as they are in part unsaturated, i. e., possess some double bond, as shown by possession of an iodine number of appreciable magnitude, or, in those cases where a detergent-forming carboxylic acid is first reacted with a poly-carboxylic acid in producing my reagent, only so long as they possess an alcoholiform hydroxyl group. also.

Instead of employing natural poly esters of reactive detergent-forming carboxylic acids in preparing my reagent, I may use synthetic esters obtained by esterifying one or more reactive detergent-forming carboxylic acids with a polyhydric alcohol of the kind heretofore recited and described in a conventional esterification reaction, such as reacting the alcohol with the acid'or acids in various molecular proportion in the presence of, for example, dry hydrogen chloride.

The compound produced by the interaction of a polyhydric alcohol of the above kind and a reactive detergent-forming carboxylic acid of the above kind will be termed a "poly ester in the present description. In all instances, itmust contain two or more radicals or residues derived from reactive detergent-forming carboxylic acids, which may be the same or different acids; and it contains one or more radicals or residues derived from polyhydric alcohols. Di-glycerides of unsaturated fatty acids are examples of poly esters, just as are the naturally-occurring tri glycerides of unsaturated fatty acids.

The reaction of elemental sulfur with such a poly ester is at first one of simple addition of sulfur at the double bond in the chain R of an acid residue in such poly ester to form a sulfurized derivative which does not differ greatly from the parent ester in properties. However, when the reaction is allowed to proceed at controlled temperatures, there is obtained a complex polymeric sulfurized product of high molecular weight, which is semi-elastic and highly viscous and which approaches the consistency of rubber, depending on the time and temperature of reaction and the proportions of reactants employed.

The nature of the chemical changes which take place is, to the best of my knowledge, not yet fully understood. I have referred above to a literature reference which suggests various mechanisms for the polymerization process. Without attempting to express exactly the composition of the reagents I employ, I desire to use those polymeric sulfurized bodies, obtained as above recited, which have a consistency short of rubber. Accordingly, I have termed them .sub-rubbery to denote a range of polymerization between the simple sulfur addition products, on one hand, and the non-usable rubbers produced on super-polymerization, on the other. Such subrubbery products are capable of dissolving in solvents to produce fluid reagents which are practicable to be used commercially.

After preparing the polymeric sub-rubbery sulfurized derivative of a poly ester of a reactive detergent-forming carboxylic acid, as above recited, I may first aminate said derivative by means of an amino-body of the following kind, or I may first react said derivative with a polycarboxylic acid of the following kind; but in all cases preparation of my reagent involves a step in which amination is effected and a step in which a poly-carboxylic acid is a reactant.

The class of alkanolamines for my purpose is characterized by the presence in the molecule of one or more alkanol or substituted alkanol groups, i. e., groups like CHzOH, CzH4OH, CaHsOH, etc. They also contain one or more amino nitrogen atoms in the molecule. The commonest examples of the class are tri-ethanolamine, di-ethanolamine, and monoethanolamine, but the class also includes, for example, ethylethanolamine, di-propanolamine, tripropanolalso have amines of the same general type in which one or more simple alkanol groups is replaced by a related group containing an ether linkage. For example, the alkanol group in the ethanolamines is CzH-rOH. Amines containing, for example, the ether-linked group are equally suited to my purpose. Similarly; the amino-bodies produced by an etherization reaction between a simple alkanolamine like an ethanolamine and a polyhydric alcohol like glycerol are suitable for my purpose so long as they retain their basic nature.

Poly-carboxylic acids include phthalic acid, oxalic acid, maleic acid, succinic'acid, citraconic acid, citric acid, glutaric acid, etc., all of which contain two or more carboxyl groups, COOH, in the molecule. I prefer to use dibasic acids having 8 carbon atomsor less. In preparing my reagent, the acid itself may be employed, or it may be preferable to employ the acid in the form of its anhydride. For example, phthalic anhydride is available at a reasonable price in a state of high technical purity. In some instances, the" anhydride shows little or no tendency to produce undesirable secondary reactions that phthalic acid shows. Therefore, in the case of phthalic acid, I have found it desirable to employ the anhydride instead of the acid in preparing my reagent. In additionto the simple poly-carboxylic acids and their anhydrides, I have found their functional equivalents, e." g., the substituted poly-carboxylic acids like chlorophthalic acid, equally useful in preparing my reagent. I

I The reagent which I use is prepared by reacting the polymeric sub-rubbery sulfurized ester of (a) a reactive detergent-forming carboxylic acid and (b) a polyhydric alcohol with an alkanola mine of the above-described kind, and with a poly-carboxylic acid of the above-described kind to produce a complex condensation product.

In preparing my preferred reagent, parts by weight of castor oil are heated to 180i C. Fifteen parts by weight of sulfur are added and the mixture is stirred continuously for 45 to 60 minutes at 188 to 190 C., or until a sample withdrawn from the reaction vessel and cooled is semi-elastic and transparent, indicating the complete absence of unreacted sulfur. To this sulfurized body there is then added 20 parts by weight of trl-ethanolamine. The temperature is reduced somewhat by such addition, but is still sufficiently high to produce the desired reaction between the sulfurized castor' oil body and the tri-ethanolamine. To this product there is then added 19 parts by weight of phthalic anhydride and heating is continued, preferably at, at least, C., until the phthalic anhydride is completely assimilated, as shown by the absence of crystals when a small sample is placed on glass and allowed tocool.

As a second exampleof a reagent which I prefer to use, the following is given: 298 parts of ricinoleic acid are mixed with 46 parts by weight of glycerol, and the mixture is agitated and heated in the presenceo'f dry hydrogen chloride gas. at a temperature in excess of 100 C. for a period of time sufficient to produce an ester. (I have found that reacting 6 hours at 'C. is satisfactory to accomplish this). If this procedure is tedious or undesirable, the di-glyceride of ricinoleic acid may be prepared in any other desired manner. For example, di-glycerides are commonly prepared by treating two mols of the triglyceride with one mol of glycerol in the presence of an alkaline catalyst. The ester so produced is mixed with 15% of its weight of. elemental sulfur, and the agitation and heating are continued until all the sulfur is assimilated and a clear transparent product is obtained, as shown by a test on glass. The product has considerable viscosity and a semi-elastic nature. This product is then mixed with 53 parts by weight of di-ethanolamine at the same temperature, 150? C., and agitation is continued for aperiod of time until the reaction is complete. Usually, heating may be discontinued on addition of the diethanolamine, the reaction being completed before the temperature has dropped very much. There is then added to the product approximately 40 parts by weight of oxalic acid. The oxalic acid should be added at as low a temperature as practicable to prevent decomposition or sublimation of said oxalic acid. I prefer to employ temperatures between 110 and 123 C.

As a third example, substitute di-olein for the di-ricinolein prepared and used in the second example just recited. (In this instance, the oxalic acid reacts through the free alcoholiform hydroxyl group of the glyceryl radical of the diolein.)

Other esters of unsaturated fatty acids or other reactive detergent-forming carboxylic acids of the kind heretofore mentioned may be used instead of the castor oil and the ricinoleic acid. For example, I have 'used cottonseed oil instead of castor oil in making certain examples of my reagent, and have found it to be useful therein. However, when cottonseed oil is used, the reaction is not as smooth as when castor oil is employed. Also, it is usually found that longer heating is required to produce the desired reagent of optimum properties. It is, therefore, preferable to use castor oil rather than cottonseed oil, so far as I am now aware. may be used instead of the tri-ethanolamine and di-ethanolamine, and other poly-carboxylic acids may be used instead of the phthalic anhydride and the oxalic acid of the above examples.

The stages of polymerization and condensation and the elastic properties of the resulting products may be altered by varying the temperature of the reaction, the time of the reaction, or the proportions of reactants employed, or any combination of these variables. I have found that the most effective reagents are those obtained by reacting 100 parts by weight of the ester with from to 17 parts by weight of sulfur, controlling the temperature to avoid the evolution of ized bodies with approximately 10 to 20 parts by' weight of phthalic anhydride.

While the foregoing description has shown products obtained by subjecting a sulfurized poly ester to the action of an alkanolamine and a poly-carboxylic acid (and particularly in that order, the poly-carboxylic acid being reacted with the aminated sulfurized body in the examples cited), I have also found that in some instances the procedure may be modified in that the poly-carboxylic acid may be reacted with the poly ester first; and the resulting product may be aminated and then sulfurized, or sulfurized and then aminated, to produce highly useful products. For example, where the poly ester contains hydroxylated detergent-forming Other alkanolamines acids like ricinoleic acid, reaction readily takes place between a carboxyl group of the polycarboxylic acid and a hydroxyl group of the hydroxylated detergent-forming acid. Also, if the poly ester contains one or more free alcoholiform hydroxyl groups from any other source, as for example the free hydroxyl group of the glyceryl radical in a di-glyceride, the poly ester will be reactive with the poly-carboxylic acid used. 1

In some instances, it may be found desirable to make the amination step the final one in the preparation of my reagent; but in general I do not find this desirable. I have found especially that if the sulfurization step be conducted after reacting the poly-carboxylic acid with the poly ester, and before the amination step, the sulfurization of the acidic poly-carboxylic-acidreacted poly ester does not proceed smoothly. There is considerable tendency to go too far in the sulfurization .step under such conditions and to produce an entirely rubbery, non-fluid product which is comparatively insoluble in solvents, and is accordingly of little or no value. However, by proceeding cautiously the operation can be conducted acceptably.

My invention, therefore, goes to the use of (l) a reagent produced by reacting a poly-carboxylic acid with an aminated poly ester which has been sulfurized before amination; (2) a reagent produced by sulfurizing a poly ester, then reacting with a poly-carboxylic acid, then aminating; (3) a reagent produced by aminating a poly ester, then sulfurizing, then reacting with a poly-carboxylic acid; (4) a reagent produced by aminating a poly ester, then reacting with a poly-carboxylic acid, then sulfurizing; (5) a reagent produced by reacting a poly ester with a poly-carboxylic acid, then sulfurizing, then aminating; and (6) a reagent produced by reacting a poly ester with a poly-carboxylic acid, then aminating, then sulfurizing. Reagents of types 5 and 6 are possible only when the poly ester has free alcoholiform hydroxyl groups, either in the reactive detergent-forming carboxylic acid residue, as in the case of ricinoleic acid, or in the glyceryl radical, as in di-glycerides. (Types 1 to 4, inclusive, may be produced from any poly ester containing the residue of an unsaturated detergent-forming acid.) The products of all these types are broadly similar, although they are not necessarily of identical structural configuration.

In other words, I have found that it is possible to prepare reagents of broadly similar composition and of equally valuable properties by varying the order of conducting thesteps of sulfurizing, aminating, and reacting the poly ester with a poly-carboxylic acid, so that in certain instances one procedure may offer advantages over the others in that it may be more adaptable to plant operations, or the product so obtained may be detectably superior to that produced by any other alternative procedure. My invention, therefore, contemplates conducting the steps of sulfurizing, aminating, and reacting a poly ester with a poly-carboxylic acid, in any desired order (subject only to the limitation, explained above, that it may not always be possible to react the poly ester and the poly-carboxylic acid as the first step in the procedure).

The final product will in some instances .exhibit a free carboxyl group, -COOI-I, depending on the proportions of poly-carboxylic acid added and the procedure employed in preparing the final product, all as recited above. Any acidity due to such free carboxyl group may be allowed to remain in the final'product, or it may be neutralized by a suitable neutralizing agent, such as a metallic hydroxide or ammonia, or by a suitable alcohol in an esterification reaction.

The products so produced are sometimes somewhat basic in character. To the extent that basicity exists in the product, it may be used in its original form, or it may be neutralized wholly or in part by reaction with a suitable acid. I have found, for example, that the acetates and the lactates prepared by reacting such basic examples of my product with acetic or lactic acid frequently have notable merit. My invention is intended to include the use of such salts, therefore.

The complex aminated poly-carboxylic-acidreacted polymeric sub-rubbery sulfurized compound obtained as recited above may be diluted with one or more solvents or diluents to improve its viscosity or other characteristics, as desired. Examples of suitable diluents are isopropanol, mineral spirits, benzol, etc.

In practising my process, the improved treating agent hereinbefore described is usually employed in the proportion of one part of reagent to from 2,000 to 20,000 parts of petroleum emulsion, either in concentrated form or after diluting as desired with a suitable vehicle or diluent or solvent. I desire to point out that the superiority of my reagent or demulsifying agent is basedon its ability to treat or break certain emulsions more advantageously and at a lower cost than is possible with other available demulsifiers or conventional mixtures thereof.

In practising my process, a reagent of the kind above described is brought into contact with or is caused to act upon the emulsion to be treated, in any of the various ways or by any of the various apparatus now generally used to resolve or break petroleum emulsions with a chemical reagent, the above procedure being used either alone or in combination with some other demulsifying procedure, such as the electrical dehydration process.

While I have described in detail the preferred embodiment of my invention, it is understood that the materials employed, the proportions of ingredients, the arrangements of steps and the details of procedure may be variously modified without departing from the spirit of the sub-.

joined claims. I

As has been pointed out, alkanolamines include those compounds in which the hydroxylated radical linked to the nitrogen atom may contain a carbon atom chain' which is interrupted by an oxygen atom, as well as the conventional type, in which there is no interruption in the carbon atom chain. Reference to a basic alkanolamine radical in the hereto appended claims is employed in this broad sense. The propriety of such broader aspect is obvious, in light of the functional equivalence previously indicated.

I claim:

1. A process for breaking petroleum emulsions of the water-in-oil type, characterized by subjecting the emulsion to the actionof a .demulsifier comprising an amino poly-carboxylic-acidreacted sub-rubbery polymeric sulfur-converted. polyhydric alcohol ester; said ester prior to sulfur-conversion containing at least 2 unsaturated high molal detergent-forming monocarboxylic acid radicals having at least 8 carbon atoms and not more than 32 carbon atoms each; said amino radical being a. basic alkanolamine radical, in which the amino nitrogen atom is free from a nitrogen-linked aryl radical.

2. A process for breaking petroleum emulsions of the water-in-oil type, characterized by subjecting the emulsion to the action of a demulsifier comprising an amino poly-carboxylic-acidreacted sub-rubbery polymeric sulfur-converted polyhydric alcohol ester; said ester prior to sulfur-conversion containing at least 2 unsaturated high molal detergent-forming monocarboxylic acid radicals having at least 8 carbon atoms and not more than 32 carbon atoms each; and said ester prior to sulfur-conversion being free from any unreacted hydroxyl radical as part of the alcoholic residue; said amino radical being a basic alkanolamine radical, in which the amino nitrogen atom is free from a nitrogen-linked aryl radical.

3. A process for breaking petroleum emulsions of the water-in-oil type, characterized by subjecting the emulsion to the action of a demulsifier comprising an amino poly-carboxylic-acidreacted sub-rubbery polymeric sulfur-converted polyhydric alcohol ester; said ester'prior to sulfur-conversion containing at least 2 unsaturated fatty acid radicals having at least 8 carbon atoms and not more than 32 carbon atoms each; and said ester prior to sulfur-conversion being free from any unreacted hydroxyl radical as part of the alcoholic residue; said amino radical being a basic alkanolamine radicaL'in which the amino nitrogen atom is free from a nitrogen-linked aryl radical.

4. A process for breaking petroleum emulsions of the water-in-oil type, characterized by sub- J'ecting the emulsion to the action of a demulsifier comprising an amino poly-carboxylic-acidreacted sub-rubbery polymeric sulfur-converted polyhydric alcohol ester; said ester prior to sulfur-conversion containing at least 2 monoethylenic fatty acid radicals having at least 8 carbon atoms and not more than 32 carbon atoms each; and said ester prior to sulfur-conversion being free from any unreacted hydroxyl radical as part of the alcoholic residue; said amino radical being a basic alkanolamine radical, in which the amino nitrogen atom is free from a nitrogenlinked aryl radical.

5. A process for breaking petroleum emulsions of the water-in-oil type, characterized by subjecting the emulsion to the action of a demulsifier comprising an amino poly-carboxylic-acid-reacted sub-rubbery polymeric sulfur-converted polyhydric alcohol ester; said ester prior to sulfur-conversion containing at least 2 radicals derived from monoethylenic fatty acids having 18 carbon atoms each; and said ester prior to sulfur-conversion being free from. any unreacted hydroxyl radical as part of the alcoholic residue;

prior to sulfur-conversion being free from any unreacted hydroxyl radical as part of the alcoholic residue; said amino radical being a basic alkanolamine radical, in which the amino nitrogen atom is free from a nitrogen-linked aryl radical.

7., A process for breaking petroleum emulsions of the water-in-oil type, characterized by subjecting the emulsion to the action of a demulsifier comprising an amino poly-carboxylicacid-reacted sub-rubbery polymeric sulfur-converted tri-ricinolein; said amino radical being a basic alkanolamine radical, inv which the amino nitrogen atom is free from a nitrogen-linked aryl radical.

8. A process for breaking petroleum emulsions of the water-in-oil type, characterized by subjecting the emulsion to the action of a demulsifier comprising a tri-ethanolamine-reacted poly-carboxylic-a'cid-reacted sub-rubbery polymeric sulfur-converted polyhydric alcohol ester; said ester prior to sulfur-conversion containing at least 2 unsaturated high molal detergent-forming monocarboxylic acid radicals having at least 8 carbon atoms and not more than 32 carbon atoms each.

9. A process-for breaking petroleum emulsions of the water-in-oil type, characterized by subjecting the emulsion to the action of a demulsifier comprising a tri-ethanolamine-reacted polycarboxylic-acid-reacted sub-rubbery polymeric sulfur-converted tri-ricinolein.

10. A process for breaking petroleum emulsions of the water-in-oil type, characterized by sub- Jecting the emulsion to the action of a demulsifier comprising a tri-ethanolamine-reacted phthalic-acid-reacted sub-rubbery polymeric sulfur-converted polyhydric alcohol ester; said ester prior to sulfur-conversion containing at least 2 unsaturated high molal detergent-forming monocarboxylic acid radicals having at least 8 carbon atoms and not more than 32 carbon atoms each. X

11. A process for breaking petroleum emulsions of the water-in-oil type, characterized by subjecting the emulsion to the action of'a demulsifier comprising a tri-ethanolamine-reacted oxalic-acid-reacted sub-rubbery polymeric sulfurconverted polyhydric alcohol ester; said ester prior to sulfur-conversion containing at least 2 converted tri-ricinolein.

. GWYNNE ALLEN. 

